An anti-tetraamination of a 1,3-diene unit via cascade annulations of the azulenone scaffold with dicarbonyl azo-compounds†
Yuhei Ishigaki,Velisoju Mahendar,Hideaki Oikawa
Chemical Communications Pub Date : 03/15/2010 00:00:00 , DOI:10.1039/B926676C
Abstract
Dense and stereo-controlled integrations of C–N bonds on the azulenone scaffold are achieved by sequential (i) ene, (ii) [6 + 2]-cycloaddition, and (iii) hetero-conjugate addition reactions leading to a topologically complex bis-bridged skeleton.